TBD Liquid Nicotine Recall [US]

TBD branded Liquid Nicotine Products

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US FlagUS/Washington: TBD Liquids LLC, of Santa Rosa, California establishment, recalls all current batch/lots (estimated to be 1,000 bottles) of TBD branded Liquid Nicotine products from the American marketplace due to reported failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, drug overdose, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/tKAD30rMLk0

Direct link: https://www.cpsc.gov/Recalls/2021/TBD-Liquids-Recalls-Liquid-Nicotine-Products-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain TBD branded Liquid Nicotine Products, as follows:

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Pro Supply Outlet Sodium, Potassium Hydroxide Recall [US]

Pro Supply Outlet Sodium, Potassium Hydroxide Recall [US]

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US FlagUS/Washington: Chemical Technologies International Inc., doing business as Pro Supply Outlet, a Rancho Cordova, California establishment, recalls an estimated 2,600 canisters of Pro Supply Outlet (“PSO”) branded Potassium Hydroxide and Sodium Hydroxide chemical products from the American marketplace due to reported failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/cb0J30rM9Je

Direct link: https://www.cpsc.gov/Recalls/2021/Pro-Supply-Outlet-Recalls-Sodium-and-Potassium-Hydroxide-Products-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-and-Violation-of-FHSA-Labeling-Requirement-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain consumer-grade Potassium Hydroxide and Sodium Hydroxide products, as follows:

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Plant Guru Wintergreen & Birch Essential Oil Recall [US]

Plant Guru Essential Oil Recall [US]

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US FlagUS/Washington: Plant Guru, a Plainfield, New Jersey establishment, recalls an estimated 25,600 bottles of Wintergreen Essential Oil, Birch Essential Oil, Headache Relief Essential Oil Blend, Headache Relief Roll-On Essential Oil Blend and Deep Muscle Essential Oil Blend from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/U8mC30rLNem

Direct link: https://www.cpsc.gov/Recalls/2021/Plant-Guru-Recalls-Wintergreen-Birch-and-Blends-of-Essential-Oils-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of Plant Guru Essential Oils, as follows:

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LifeSeasons Blood Nourish-R Supplement Recall [US]

LifeSeasons Blood Nourish-R Supplement Recall [US]

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US FlagUS/Washington: LifeSeasons Inc., a Springville, Utah establishment, recalls an estimated 7,800 bottles of LifeSeasons Blood Nourish-R Supplements from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/I2l030rLH8e

Direct link: https://www.cpsc.gov/Recalls/2021/UST-Recalls-Bottles-of-LifeSeasons-Blood-Nourish-R-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain LifeSeasons Blood Nourish-R Supplements marketed, sold and delivered in the United States, as follows:

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The Lye Guy Potassium, Sodium Hydroxide Recall [US]

The Lye Guy Sodium Hydroxide and Potassium Hydroxide Recall [US]

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US FlagUS/Washington: The Lye Guy, a Pennellville, New York establishment, recalls an estimated 32,000 canisters of Potassium Hydroxide and Sodium Hydroxide chemical products from the American marketplace due to reported failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/xOQH30rL6Wz

Direct link: https://www.cpsc.gov/Recalls/2021/The-Lye-Guy-Recalls-Sodium-and-Potassium-Hydroxide-Products-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-and-Violation-of-FHSA-Labeling-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain consumer-grade The Lye Guy Potassium Hydroxide and Sodium Hydroxide products, as follows:

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Welmate Lidocaine Numbing Cream Recall [US]

Welmate Lidocaine Numbing Cream Recall [US]

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US FlagUS/Washington: YYBA Corp., doing business as Wellspring, a Monsey, New York establishment, recalls an estimated 15,000 jars of Welmate Lidocaine Numbing Cream from the American marketplace due to failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/DH9A30rGou9

Direct link: https://www.cpsc.gov/Recalls/2021/YYBA-Recalls-Welmate-Lidocaine-Numbing-Cream-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves Welmate Lidocaine Numbing Cream marketed, sold and delivered in the United States, as follows:

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dōTERRA Deep Blue & PastTense Essential Oil Recall [US]

dōTERRA Deep Blue & PastTense Essential Oil Recall [US]

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US FlagUS/Washington: dōTERRA International LLC, a Pleasant Grove, Utah establishment, recalls an estimated 1.3 million Deep Blue, PastTense and Deep Blue Touch branded Essential Oil products from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/H6CC30rFXd8

Direct link: https://www.cpsc.gov/Recalls/2021/doTERRA-Recalls-1-3-Million-Bottles-of-Deep-Blue-PastTense-and-Deep-Blue-Touch-Essential-Oils-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain dōTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils in 10 mL glass bottles with rollerball applicator and black cap, as follows:

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Scalpa Numb Anesthetic Cream Recall [US]

Scalpa Numb Anesthetic Cream Recall [US]

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US FlagUS/Washington: Scalpa Inc., a Phoenix, Arizona establishment, recalls an estimated 10,000 tubes of Scalpa Numb Maximum Strength Topical Anesthetic Cream from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/Jf6430rt21h

Direct link: https://www.cpsc.gov/Recalls/2021/Scalpa-Recalls-Scalpa-Numb-Maximum-Strength-Topical-Anesthetic-Cream-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves Scalpa Numb Maximum Strength Topical Anesthetic Cream marketed, sold and delivered in the United States, as follows:

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Excedrin Migraine & Headache Medication Recall [US]

Excedrin Migraine & Headache Caplets

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US FlagUS/Washington: GSK Consumer Healthcare, a Warren, New Jersey establishment, recalls an estimated 433,600 bottles of Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets and Excedrin Tension Headache Caplets from the American marketplace due to reported packaging defects and consequential failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act with resultant risks of child poisoning, overdose, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/O4Qd30rqgVO

Direct link: https://www.cpsc.gov/Recalls/2021/GSK-Consumer-Health-Recalls-Five-Excedrin-Brands-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of Excedrin Migraine and Headache Medications, as follows:

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Crafty Bubbles Wintergreen Essential Oil Recall [US]

US FlagUS/Washington: Crafty Bubbles Wintergreen Essential Oil Recall [US]Bolek’s Craft Supplys Inc., a Dover, Ohio establishment, recalls an estimated 5,600 bottles of Crafty Bubbles Wintergreen Essential Oil products from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/UQWZ30rjMds

Direct link: https://www.cpsc.gov/Recalls/2021/Boleks-Craft-Supplys-Recalls-Wintergreen-Essential-Oil-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of  Wintergreen Essential Oils, as follows:

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Rocky Mountain Wintergreen Essential Oil Recall [US]

Rocky Mountain Wintergreen Essential Oil Recall [US]

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US FlagUS/Washington: Rocky Mountain Oils, an Orem, Utah establishment, recalls an estimated 33,000 bottles of Wintergreen Essential Oils and Oil Blends from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/DEor30ricUa

Direct link: https://www.cpsc.gov/Recalls/2021/Rocky-Mountain-Oils-Recalls-Wintergreen-Essential-Oil-and-Oil-Blends-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of  Wintergreen Essential Oils, as follows:

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Organic Aromas Wintergreen Essential Oil Recall [US]

13631 - CPSC - Organic Aromas Wintergreen Essential Oil Recall [US]

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US FlagUS/Washington: Organic Aromas LLC, a Boise, Idaho establishment, recalls an estimated 300 Organic Aromas Wintergreen Essential Oils from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/ow1Q30rf0XR

Direct link: https://www.cpsc.gov/Recalls/2020/Organic-Aromas-Recalls-Wintergreen-Essential-Oil-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Organic Aromas Wintergreen Essential Oil products sold and delivered in amber glass bottles with white or black caps, as follows:

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Autozone, Highline & Prestone Antifreeze Recall [US]

Autozone, Highline & Prestone Antifreeze Recall [US]

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US FlagUS/Washington: Prestone Products Corporation, a Rosemont, Illinois establishment, recalls an estimated 687,000 bottles of Autozone, Highline, Prestone, Starfire and Supertech branded Antifreeze products from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/YipP30rdPS0

Direct link: https://www.cpsc.gov/Recalls/2021/Prestone-Products-Recalls-Antifreeze-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of Antifreeze products, as follows (in alphabetical order):

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Vitamin Shoppe Vthrive Bioactive Multivitamin Recall [US]

Vitamin Shoppe Vthrive Bioactive Multivitamin Recall [US]

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US FlagUS/Washington: The Vitamin Shoppe, a Secaucus, New Jersey establishment, recalls an estimated 8,200 bottles of Vthrive Bioactive Multivitamins from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/X2WJ30rcqVr

Direct link: https://www.cpsc.gov/Recalls/2020/The-Vitamin-Shoppe-Recalls-Vthrive-Bioactive-Multivitamins-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of Multivitamins, as follows:

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Medi-First, Medique, Dover, Otis Clapp & Ecolab Med Recall

Medi-First, Medique, Dover, Otis Clapp & Ecolab Med Recall

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US FlagUS/Washington: Medique, a Fort Myers, Florida establishment, recalls an estimated 143,300 Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp and Ecolab branded medications and/or health products from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/aPaY30r9OOg

Direct link: https://www.cpsc.gov/Recalls/2020/Medique-Recalls-31-Different-Over-the-Counter-Drugs-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Sold-Exclusively-on-Amazon-com-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports the recall involves 31 different over-the-counter drugs purchased on or after June 1, 2018 that are unexpired from the following brands: Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp and Ecolab, as follows (in alphabetical order):

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